Canonical Allele Identifier: CA363504039

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007389T>G (hg19) ; chr6:g.32039612T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039612T>G , CM000668.2:g.32039612T>G	GRCh38
NC_000006.11:g.32007389T>G , CM000668.1:g.32007389T>G	GRCh37
NC_000006.10:g.32115368T>G	NCBI36
NG_007941.2:g.6305T>G
NG_008337.2:g.74763A>C
NG_007941.3:g.6308T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.616T>G MANE Select	ENSP00000496625.1:p.Ser206Ala
ENST00000418967.6:c.616T>G	ENSP00000408860.2:p.Ser206Ala
ENST00000435122.3:c.526T>G	ENSP00000415043.2:p.Ser176Ala
ENST00000462278.1:n.204T>G
ENST00000464325.5:n.537T>G
ENST00000466779.5:c.*308T>G	ENSP00000417321.1:n.*308T>G
ENST00000466879.5:n.667T>G
ENST00000469053.5:c.*308T>G	ENSP00000418104.1:n.*308T>G
ENST00000479074.5:n.674T>G
ENST00000479730.5:n.732T>G
ENST00000483041.5:n.785T>G
ENST00000486063.5:n.796T>G
NM_000500.7:c.616T>G	NP_000491.4:p.Ser206Ala
NM_001128590.3:c.526T>G	NP_001122062.3:p.Ser176Ala
XM_011514314.1:c.211T>G	XP_011512616.1:p.Ser71Ala
NM_000500.9:c.616T>G MANE Select	NP_000491.4:p.Ser206Ala
NM_001368143.1:c.211T>G	NP_001355072.1:p.Ser71Ala
NM_001368144.1:c.211T>G	NP_001355073.1:p.Ser71Ala
NM_001128590.4:c.526T>G	NP_001122062.3:p.Ser176Ala
NM_001368143.2:c.211T>G	NP_001355072.1:p.Ser71Ala
NM_001368144.2:c.211T>G	NP_001355073.1:p.Ser71Ala